ClinVar Miner

List of variants reported for Spermatogenic failure 46 by Fulgent Genetics, Fulgent Genetics

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001206927.2(DNAH8):c.8339T>C (p.Ile2780Thr) rs142328376 0.00463
NM_001206927.2(DNAH8):c.4908G>T (p.Glu1636Asp) rs61757219 0.00440
NM_001206927.2(DNAH8):c.11776T>C (p.Leu3926=) rs148084212 0.00168
NM_001206927.2(DNAH8):c.13823C>T (p.Thr4608Met) rs142438011 0.00168
NM_001206927.2(DNAH8):c.7471A>G (p.Ile2491Val) rs148698911 0.00101
NM_001206927.2(DNAH8):c.7123A>C (p.Asn2375His) rs141532428 0.00092
NM_001206927.2(DNAH8):c.7774C>T (p.Arg2592Trp) rs113332942 0.00064
NM_001206927.2(DNAH8):c.14059C>T (p.Arg4687Ter) rs146551804 0.00058
NM_001206927.2(DNAH8):c.11701G>A (p.Ala3901Thr) rs560568324 0.00050
NM_001206927.2(DNAH8):c.4303-15T>C rs201364154 0.00048
NM_001206927.2(DNAH8):c.725G>A (p.Arg242His) rs142863013 0.00021
NM_001206927.2(DNAH8):c.2980A>T (p.Ile994Leu) rs141818413 0.00019
NM_001206927.2(DNAH8):c.13417A>C (p.Ile4473Leu) rs200416428 0.00011
NM_001206927.2(DNAH8):c.6434A>G (p.Gln2145Arg) rs780541458 0.00009
NM_001206927.2(DNAH8):c.9025C>A (p.Leu3009Met) rs199779645 0.00008
NM_001206927.2(DNAH8):c.3377G>A (p.Arg1126His) rs776311330 0.00006
NM_001206927.2(DNAH8):c.11345A>C (p.Asn3782Thr) rs150057448 0.00004
NM_001206927.2(DNAH8):c.8747+4C>T rs201261721

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